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Year : 2012  |  Volume : 1  |  Issue : 3  |  Page : 123-126

Congenital Cystic Adenomatoid Malformation

Correspondence Address:
Varsha H Chauhan

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Source of Support: None, Conflict of Interest: None

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CCAM is a rare congenital lung malformation representing 25% of congenital malformations and 95% of congenital lung lesions.(1) CCAM may be diagnosed in utero by ultrasound examination, or after birth with the presentation of respiratory distress like symptoms. Most CCAM lesions are manageable with the proper assessment, diagnosis, and interventions.

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